LFP as initiator of in-battery polymerization of conducting polymers for high-rate-charging cathodes

ABSTRACT

Cathodes for a fast charging lithium ion battery, processes for manufacturing thereof and corresponding batteries are provided. Cathode formulations comprise spinel and/or layered structure cathode material with 5-10% of cathode material having an olivine-based structure as polymerization initiator, binder material, and monomer and/or oligomer material selected to polymerize into a conductive polymer upon partial delithiation of the olivine-based structure cathode material during at least a first charging cycle of a cell having a cathode made of the cathode formulation. When the cathode is used in a battery, polymerization is induced in-situ (in-cell) during first charging cycle(s) of the battery to provide a polymer matrix which is evenly dispersed throughout the cathode.

CROSS REFERENCE TO RELATED APPLICATIONS

This application is a Continuation-in-part of U.S. application Ser. No. 15/686,788, filed on Aug. 25, 2017, which is a continuation of U.S. application Ser. No. 15/434,083, filed on Feb. 16, 2017, now U.S. Pat. No. 9,831,488, which claims the benefit of U.S. Provisional Patent Application No. 62/432,588, filed Dec. 11, 2016, all of which are hereby incorporated by reference.

BACKGROUND OF THE INVENTION 1. Technical Field

The present invention relates to the field of batteries, and more particularly, to cathodes for fast charge lithium ion batteries.

2. Discussion of Related Art

Rechargeable lithium batteries are extensively used for portable electronic devices as well as hybrid electronic vehicles. The cell capacity and rate capability as well as safety, environmental compatibility, life cycle, and cost are among the commercial considerations in preparing and using various types of batteries. The olivine LiFePO₄ (LFP) cathode material is known to be low-cost, safe, environmentally benign, and further, provides beneficial cyclability and large capacity at high rates of charge and discharge. It is noted that the LFP particles used are of nano-scale and/or are coated with carbon; due to poor kinetic response of electronic and Lit-ion transfer under rapid-rate conditions.

SUMMARY OF THE INVENTION

The following is a simplified summary providing an initial understanding of the invention. The summary does not necessarily identify key elements nor limit the scope of the invention, but merely serves as an introduction to the following description.

One aspect of the present invention provides a cathode, prepared from a cathode formulation comprising: cathode material having spinel or layered structure, up to 10 wt % cathode material having an olivine-based structure, binder material, and monomer and/or oligomer material selected to polymerize into a conductive polymer upon partial delithiation of the olivine-based structure cathode material during at least a first charging cycle of a cell having the cathode, wherein: the monomer and/or oligomer material is in monomer and/or oligomer form in the cathode in its pristine form prior to the first charging cycle of the cell, the partial delithiation is carried out electrochemically during the first charging cycle of the cell, and following the first charging cycle of the cell, the monomer and/or oligomer material is at least partly polymerized.

These, additional, and/or other aspects and/or advantages of the present invention are set forth in the detailed description which follows; possibly inferable from the detailed description; and/or learnable by practice of the present invention.

BRIEF DESCRIPTION OF THE DRAWINGS

For a better understanding of embodiments of the invention and to show how the same may be carried into effect, reference will now be made, purely by way of example, to the accompanying drawings in which like numerals designate corresponding elements or sections throughout.

In the accompanying drawings:

FIGS. 1 and 7 are high level schematic illustrations of cathode formulations, cathodes and cells, according to some embodiments of the invention.

FIGS. 2A-2C illustrate examples for a prior art charging curve (FIG. 2A), a first cycle of a charging curve of the pristine cell with the pristine cathode having pyrrole monomers as monomer and/or oligomer material (FIG. 2B), and a potential curve of the pristine cathode having pyrrole monomers as monomer and/or oligomer material which is surface polymerized outside cell, as comparison (FIG. 2C), according to some embodiments of the invention.

FIG. 3 is an illustration of an experimental comparison of cells with disclosed cathodes, with prior art cells having cathodes that lack the monomers, according to some embodiments of the invention.

FIG. 4 is an illustration of an experimental comparison of cathodes having pyrrole as monomer and/or oligomer material versus cathodes having aniline as monomer and/or oligomer material, according to some embodiments of the invention.

FIGS. 5A-5J are high resolution scanning electron microscope (HRSEM) images comparing prior art cathodes with pristine and operative cathodes respectively, according to some embodiments of the invention.

FIG. 6 is a high level schematic illustration of a method, according to some embodiments of the invention.

DETAILED DESCRIPTION OF THE INVENTION

In the following description, various aspects of the present invention are described. For purposes of explanation, specific configurations and details are set forth in order to provide a thorough understanding of the present invention. However, it will also be apparent to one skilled in the art that the present invention may be practiced without the specific details presented herein. Furthermore, well known features may have been omitted or simplified in order not to obscure the present invention. With specific reference to the drawings, it is stressed that the particulars shown are by way of example and for purposes of illustrative discussion of the present invention only, and are presented in the cause of providing what is believed to be the most useful and readily understood description of the principles and conceptual aspects of the invention. In this regard, no attempt is made to show structural details of the invention in more detail than is necessary for a fundamental understanding of the invention, the description taken with the drawings making apparent to those skilled in the art how the several forms of the invention may be embodied in practice.

Before at least one embodiment of the invention is explained in detail, it is to be understood that the invention is not limited in its application to the details of construction and the arrangement of the components set forth in the following description or illustrated in the drawings. The invention is applicable to other embodiments that may be practiced or carried out in various ways as well as to combinations of the disclosed embodiments. Also, it is to be understood that the phraseology and terminology employed herein is for the purpose of description and should not be regarded as limiting.

It is noted that the disclosed general formulas relate to the stoichiometry of the material, which may vary by a few percent from the stoichiometry due to substitution or other defects present in the structure.

Cathodes for a fast charging lithium ion battery, processes for manufacturing thereof and corresponding batteries are provided. Cathode formulations comprise spinel and/or layered structure cathode material (or mixture of thereof, and possibly mixtures thereof with olivine cathode material), 5-10% of cathode material having an olivine-based structure as polymerization initiator, binder material, and monomer and/or oligomer material selected to polymerize into a conductive polymer upon partial delithiation of the olivine-based structure cathode material during at least a first charging cycle of a cell having a cathode made of the cathode formulation. When the cathode is used in a battery, polymerization is induced in-situ (in-cell) during first charging cycle(s) of the battery to provide a polymer matrix which is evenly dispersed throughout the cathode.

FIGS. 1 and 7 are high level schematic illustrations of cathode formulations 100, cathodes 110, 115 and cells 120, 125, according to some embodiments of the invention. In FIG. 1 the cathode material is based on cathode material having an olivine-based structure, while in FIG. 7 the cathode material is based on cathode material having a spinel-based and/or layered structure, with olivine-based structure cathode material in small amount (up to 10 wt %) to initiate in-situ polymerization of the monomer and/or oligomer material, as described below.

Cathode formulations 100 (see e.g., FIG. 1) may comprise cathode material 90 having an olivine-based structure (and optional additives, see below), binder material 98, and monomer and/or oligomer material 95 selected to polymerize into a conductive polymer upon partial delithiation of cathode material 90 during at least a first charging cycle of cell 120, 125 having cathode 110, 115 made of cathode formulation 100. Pristine cathode 110 and pristine cell 120 denote for example cathodes and cells prior to their first charging cycle, while cathode 115 and operating cell 125 denote for example cathodes and cells after their first charging cycle has been carried out. Dried cathode slurries made of cathode formulations 100 are likewise part of the present disclosure. It is noted that similar configurations may be applied to other electrodes and are shown here for cathodes as a non-limiting example.

Cathode formulations 100 (see e.g., FIG. 7) may comprise cathode material 91 having spinel-based and/or layered structure, 5-10 wt % of cathode material 90 having an olivine-based structure (and optional additives, see below), binder material 98, and monomer and/or oligomer material 95 selected to polymerize into a conductive polymer upon partial delithiation of olivine-based structure cathode material 90 during at least a first charging cycle of cell 120, 125 having cathode 110, 115 made of cathode formulation 100. Pristine cathode 110 and pristine cell 120 denote for example cathodes and cells prior to their first charging cycle, while cathode 115 and operating cell 125 denote for example cathodes and cells after their first charging cycle has been carried out. Dried cathode slurries made of cathode formulations 100 are likewise part of the present disclosure. It is noted that similar configurations may be applied to other electrodes and are shown here for cathodes as a non-limiting example.

Cathode formulations 100 in any of the embodiments may comprise (olivine-based structure) cathode material 90 consisting of A_(z)MXO₄, wherein A is Li, alone or partially replaced by at most 10% of Na and/or K; 0≤z≤1; M is at least 50% of Fe(II) or Mn(II) or mixture thereof; and XO₄ is PO₄, alone or partially replaced by at most 10 mol % of at least one group selected from SO₄ and SiO₄. For example, cathode material 90 may include LFP (LiFePO₄) cathode material. Cathode material 90 may further comprise additives such as conductive materials, e.g., carbon black and/or carbon nano-tubes. Cathode formulations 100 may comprise a carbon coating. Spinel-based and/or layered structure cathode material 91 may consist of at least one of: LCO formulations (based on LiCoO₂), NMC formulations (based on lithium nickel-manganese-cobalt), NCA formulations (based on lithium nickel cobalt aluminum oxides), LMO formulations (based on LiMn₂O₄) and LMN formulations (based on lithium manganese-nickel oxides).

In certain embodiments M may be selected from Fe(II), Mn(II) and mixtures thereof, alone or partially replaced by at most 50% of one or more other metals selected from Ni and Co and/or by at most 15% of one or more aliovalent or isovalent metals other than Ni or Co, and/or by at most 5% as atoms of Fe(III).

In certain embodiments, M may be selected from Fe(II), Mn(II) and mixtures thereof, alone or partially replaced by at most 50% of one or more other metals chosen from Ni and Co and/or by at most 15% as atoms of one or more aliovalent or isovalent metals selected from Mg, Mo, Nb, Ti, Al, Ta, Ge, La, Y, Yb, Cu, Sm, Ce, Hf, Cr, Zr, Bi, Zn, Ca, B and W and/or by at most 5% as atoms of Fe(III).

In certain embodiments, cathode material 90 may comprise a compound corresponding to the general formula Li_(z)Fe_(y)Mn_(1-y)PO₄ which has an olivine structure, wherein z and y are each independently between 0 and 1 (e.g., A may be Li, M may be Fe_(y)Mn_(1-y), X may be P, 0≤z≤1, 0≤y≤1, independently).

Cathode formulations 100 may comprise monomer and/or oligomer material 95 consisting of monomers of any of pyrrole, aniline, thiophene, phenyl mercaptan, furan, and phenol. In certain embodiments, monomer and/or oligomer material 95 may comprise oligomers, at least as part of monomer and/or oligomer material 95. In certain embodiments, monomer and/or oligomer material 95 may consist of oligomers. In certain embodiments, monomer and/or oligomer material 95 may consist of monomers. In certain embodiments, monomer and/or oligomer material 95 may comprise ethylenedioxythiophene and styrenesulfonate which may polymerize to conductive polymer PEDOT-PSS (Poly(3,4-ethylenedioxythiophene)-poly(styrenesulfonate) upon partial delithiation of cathode material 90 during at least a first charging cycle of cell 120, 125. In certain embodiments, monomer and/or oligomer material 95 may comprise combinations of monomers and/or oligomers. In certain embodiments, the rings in any of the monomer embodiments may be substituted with one or more straight, branched or bridged alkyl, alkenyl, oxa-alkyl, oxa-alkenyl, aza-alkyl, aza-alkenyl, thia-alkyl, thia-alkenyl, sila-alkyl, sila-alkenyl, aryl, aryl-alkyl, alkyl-aryl, alkenyl-aryl, dialkylamino and dialkylazo compounds comprising about 1-30 carbon atoms.

Cathode formulations 100 may comprise binder material 98 such as carboxymethyl cellulose (CMC), polyvinylidene difluoride (PVDF), polyacrylic acid (PAA), polyethylene oxide (PEO), polyvinyl alcohol (PVA) and/or alginate as non-limiting examples.

Some embodiments comprise cathode formulations 100 having 80-90% of cathode material 90, 1-10% of binder material 98 and 1-10% of monomer and/or oligomer material 95. Some embodiments comprise cathode formulations 100 having 90-98% of cathode material 90, 1-5% of binder material 98 and 1-5% of monomer and/or oligomer material 95. In certain embodiments, cathode formulations 100 may comprise more than 90% of cathode material 90. In certain embodiments, cathode formulations 100 may comprise more than 10% of binder material 98. In certain embodiments, cathode formulations 100 may comprise more than 10% of monomer and/or oligomer material 95. Some embodiments comprise any sub-range of weight % combinations within the disclosed ranges.

Some embodiments comprise cathode formulations 100 having 70-90% of cathode material 91, 5-10% of olivine-based structure cathode material 90, 1-10% of binder material 98 and 1-10% of monomer and/or oligomer material 95. Some embodiments comprise cathode formulations 100 having 90-98% of cathode material 90, 1-5% of binder material 98 and 1-5% of monomer and/or oligomer material 95. In certain embodiments, cathode formulations 100 may comprise between 85%-93% of cathode material 91 and 5% of olivine-based structure cathode material 90. In certain embodiments, cathode formulations 100 may comprise more than 10% of binder material 98. In certain embodiments, cathode formulations 100 may comprise more than 10% of monomer and/or oligomer material 95. Some embodiments comprise any sub-range of weight % combinations within the disclosed ranges.

Cells 120, 125 may comprise cathodes 110, 115 prepared from cathode formulations 100, as well as an anode, electrolyte and a separator (illustrated collective and schematically by a member 80 in the cell). Pristine cathode 110 is prepared from cathode formulations 100, e.g., by spreading and drying, with cathode material 90 having an olivine-based structure, binder material 98, and monomer and/or oligomer material 95, while cathode 115 has a conductive polymer formed during at least a first charging cycle of cell 120, 125 from monomer and/or oligomer material 95. Without being bound by theory, it is suggested that the polymerization of monomer and/or oligomer material 95 into the conductive polymer is carried out upon partial delithiation of cathode material 90 during the first cycle(s) of charging and discharging cell 120, 125. As the polymerization probably occurs during first charging cycle(s), it is referred to herein as in-situ, or in-cell polymerization, in contrast to prior art cathodes which are polymerized before being incorporated in operating cell 125.

In cathodes according to some embodiments of the invention, the monomer and/or oligomer material may be either in monomer and/or oligomer form or at least partially polymerized depending on whether a first charging cycle of the cell has taken place. The monomer and/or oligomer material may be in monomer and/or oligomer form in the cathode in its pristine form prior to the first charging cycle of the cell, the partial delithiation may be carried out electrochemically during the first charging cycle of the cell, and, following the first charging cycle of the cell, the monomer and/or oligomer material may be at least partly polymerized.

Without being bound by theory, an indication to the occurrence of the polymerization process during the charging process is illustrated schematically by peak 113 in FIGS. 1 and 7, and is further illustrated in examples provided in FIGS. 2A-2C. FIGS. 2A-2C illustrate examples for a prior art charging curve 85 (FIG. 2A), a first cycle of a charging curve 130 of pristine cell 120 with pristine cathode 110 having pyrrole monomers as monomer and/or oligomer material 95 (FIG. 2B) and a potential curve 130A of pristine cathode 110 having pyrrole monomers as monomer and/or oligomer material 95 which is surface electro-polymerized outside cell 120 (FIG. 2C), as comparison, according to some embodiments of the invention. While in prior art charging 85 the measured cathode potential is monotonous after the initial rise, charging curve 130 shows a clear local peak 113 in the potential at around 3.465V which is understood as corresponding to the polymerization of monomer and/or oligomer material 95 in cathode 110 in cell 120 during actual charging, once sufficient partial delithiated cathode material has formed during the charging, as indicated by the potential value. This understanding was corroborated by identifying a peak 113A at a similar potential value under surface polymerization of pyrrole monomers on another cathode 110 outside cell 120. The inventors suggest that, without being bound by theory, local peak 113 in charging curve 130 indicates the specified potential which corresponds to a polymerization reaction of monomer and/or oligomer material 95 in presence of the partially delithiated cathode material (e.g., by oxidation). It is noted that peak 113 is reduced and/or vanishes in later cycles, probably due to the completion of the polymerization. In different experiments, local peak 113 was found between 3.455V-3.465V. It is noted that cathodes 115 may be made operable by polymerization of monomer and/or oligomer material 95 during the first cycle(s) even if local peak 113 is not visible on the charging curve, possibly due to cycling conditions and cathode composition. The presence of peak 113 is merely understood as a non-limiting indicator of the polymerization process, and not as a required condition thereto.

FIG. 3 is an illustration of an experimental comparison of cells 125 with disclosed cathode 115 with prior art cells having cathodes that lack the monomers, according to some embodiments of the invention. The cell capacity and cyclability are exemplified at charging/discharging rates of 0.1 C, 1 C, 5 C, 10 C and 15 C, illustrating the superior capacity of cells 125, particularly at high charging rates such as 15 C in which cells 125 achieved more than threefold the capacity of prior art cells (indicated by A in the figure).

FIG. 4 is an illustration of an experimental comparison of cathodes 115 having pyrrole as monomer and/or oligomer material 95 versus cathodes 115 having aniline as monomer and/or oligomer material 95, according to some embodiments of the invention. In both cases, monomer and/or oligomer material 95 was added as 5% (weight %) of the cathode slurry and both cases show high capacities in all charging rates, and particularly at high charging rates such as 5 C, 10 C, 15 C and possibly higher charging rates.

FIGS. 5A-5J are high resolution scanning electron microscope (HRSEM) images comparing prior art cathodes 86A, 86B with pristine and operative cathodes 110, 115, respectively, according to some embodiments of the invention. FIGS. 5A and 5C show surface HRSEM images of pristine prior art cathodes 86A (LFP) and 86B (LFP with polypyrrole, polymerized prior to the first cycle, added polymerized into the cathode slurry), respectively, and FIG. 5B is a surface HRSEM image of pristine cathode 110 (in the illustrated non-limiting example, LFP with pyrrole monomer material 95). FIGS. 5D and 5F show cross section HRSEM images of pristine prior art cathodes 86A and 86B, respectively, and FIG. 5E is a cross section HRSEM image of pristine cathode 110. FIGS. 5G and 5I show surface HRSEM images of operative cathode 115 and prior art cathode 86B, respectively. FIGS. 5H and 5J show cross section HRSEM of operative cathode 115 and prior art cathode 86B, respectively. Advantageously, the inventors have found out that the disclosed in-cell polymerization of monomer and/or oligomer material 95 yields thick and uniform polymerization of polypyrrole through the whole cross section of electrode 115 (FIG. 5H), in stark contrast to prior art electrode 86B (FIG. 5J).

FIG. 6 is a high level schematic illustration of a method 200, according to some embodiments of the invention. The method stages may be carried out with respect to cathode formulations 100, cathodes 110, 115 and cells 120, 125 described above, which may optionally be configured to implement method 200. Method 200 may comprise stages for producing, preparing and/or using device cathode formulations 100, cathodes 110, 115 and cells 120, 125 described above, such as any of the following stages, irrespective of their order.

Method 200 may comprise configuring an olivine-based cathode for in-situ (in-cell) polymerization (stage 210), e.g., by selecting monomers which polymerize into a conducting polymer in presence of partially delithiated olivine-based cathode material (stage 215), adding the monomers to the cathode material (stage 220) configuring the cathode to undergo the polymerization during the first charging cycle(s) (stage 225), e.g., polymerizing the monomers during the first charging cycle(s) (stage 230) and producing the operative cathode in-situ by the polymerization (stage 240).

In certain embodiments, method 100 may further comprise adding up to 10% olivine-based structure cathode material to cathode material having spinel and/or layered structure (stage 205). In certain embodiments, cathode(s) 87 may comprise materials based on layered, spinel and/or olivine frameworks, and with up to 10 wt % of LFP formulations (based on LiFePO₄) with Fe possibly partly replaced by Mn as disclosed above and 90 wt % or more of any of various spinel and/or layered structure compositions, such as LCO formulations (based on LiCoO₂), NMC formulations (based on lithium nickel-manganese-cobalt), NCA formulations (based on lithium nickel cobalt aluminum oxides), LMO formulations (based on LiMn₂O₄), LMN formulations (based on lithium manganese-nickel oxides), lithium rich cathodes, and/or combinations thereof.

In certain embodiments, cathode material 90 consists of A_(z)MXO₄, wherein A is Li, alone or partially replaced by at most 10% of Na and/or K; 0≤z≤1, M may be selected from Fe(II), Mn(II) and mixtures thereof, alone or partially replaced by at most 50% of one or more other metals selected from Ni and Co and/or by at most 15% of one or more aliovalent or isovalent metals other than Ni or Co, and/or by at most 5% as atoms of Fe(III) and XO₄ is PO₄, alone or partially replaced by at most 10 mol % of at least one group selected from SO₄ and SiO₄.

In certain embodiments, M may be selected from Fe(II), Mn(II) and mixtures thereof, alone or partially replaced by at most 50% of one or more other metals chosen from Ni and Co and/or by at most 15% as atoms of one or more aliovalent or isovalent metals selected from Mg, Mo, Nb, Ti, Al, Ta, Ge, La, Y, Yb, Cu, Sm, Ce, Hf, Cr, Zr, Bi, Zn, Ca, B and W and/or by at most 5% as atoms of Fe(III).

In certain embodiments, cathode material 90 may comprise a compound corresponding to the general formula Li_(z)Fe_(y)Mn_(1-y)PO₄ which has an olivine structure, wherein z and y are each independently between 0 and 1 (e.g., A may be Li, M may be Fe_(y)Mn_(1-y), X may be P, 0≤z≤1, 0≤y≤1, independently).

In certain embodiments, cathode material 90 may comprise a compound corresponding to the general formula Li_(z)FePO₄ which has an olivine structure, wherein 0≤z≤1 (e.g., with M as Fe).

In certain embodiments, cathode material 90 may be a partially delithiated polymerization initiator with the formula C-A_(z)MXO₄, having on at least a portion of a surface thereof, a film of carbon (e.g., deposited by pyrolysis, as an additive to cathode material 90, coated on the surface, etc.). The film of carbon may be uniform, adherent and non-powdery. The film of carbon may be up to 15% of a weight of the polymerization initiator, or between 0.5%-5% of a weight of the polymerization initiator.

According to some embodiments, when the cathode is used in a battery comprising a current collector, a first charging cycle of the cathode causes polymerization initiator molecules (e.g., the partially delithiated A_(z)MXO₄) to induce polymerization of monomer and/or oligomer material 95 incorporated in cathode 110, thereby providing a polymer matrix between cathode material 90 and the current collector (not shown) to which cathode 110 is attached. According to some embodiments, the polymerization process which occurs within the cathode may provide a polymer that is evenly dispersed throughout the cathode.

Introduction of electrochemically-active conducting polymers such as polypyrrole (PPy) and polyaniline (PAni) into LFP/C-LFP composite cathodes is known to enhance both the capacity and rate capability. The conductive polymers appear to provide good electronic contact between active particles themselves and with the current collector, and acts as a host material for Li⁺ insertion/extraction. It has also been shown that the Li⁺ diffusivity is greatly enhanced probably due to electrostatic attraction between the anions of the conducting polymer and Li⁺ which can help Li⁺ pull out of LFP particles. However, in the prior art, solutions concerning the incorporation of the conductive polymer are insufficiently effective or are industrially inapplicable. For example, prior art methods for preparing such composite cathodes include: (i) oxidative polymerization of the monomer in solution containing suspended oxide powders, wherein the prepared PPy-LFP particles are mixed with a binder and carbon to prepare the cathode; (ii) conventional fabrication by mixing the formerly synthesized polymer with oxide and the inactive additives (carbon and binder). The polymer can be synthesized chemically or electrochemically using the monomer as-is or following chemical modification for covalently attaching a redox couple, such as ferrocene; (iii) in-situ electrodeposition onto designated current collector (e.g., stainless-steel mesh) from suspension containing oxide particles and a monomer in an organic solvent (e.g., acetonitrile) via cyclic voltammetry—the resulted cathode may be used as-is without any additional binder or additives; (iv) in-battery electro-polymerization an LFP cathode is closed in a coin-cell in the presence of a monomer dissolved in an electrolyte and the polymer is polymerized by either a single step of charging to induce de-lithiation of the cathode or by initial charge to induce de-lithiation followed by the addition of a monomer solution after which an additional galvanostatic step is performed to complete the polymerization, wherein the partially delithiated lithium metal phosphate acts as a polymerization initiator.

Advantageously, while prior art polymerization is carried out prior to the preparation of the cathode or prior to the insertion of the cathode into the cell, and typically from compound in the electrolyte or in a solution, disclosed cathodes 110 are prepared from slurries which include monomer and/or oligomer material 95 and polymerization is carried out in cell 120, 125 without need for separate polymerization of monomer and/or oligomer material 95 during the preparation of cathode 110, before introducing cathode 100 into cell 120. The disclosed invention thus provides significant process advantages as well as superior cathodes and cells, as explained above.

In certain embodiments, the cathode may be made by preparing an electrode slurry composition by dispersing the electrode active material, a binder, a conductive material and a thickener, if desired, in a solvent and coating the slurry composition on an electrode collector. As non-limiting examples, aluminum or aluminum alloy may be used as a current collector. The current collector may be formed as a foil or mesh. In any of the disclosed embodiments, anodes may comprise anode active material particles such as graphite, graphene or other carbon-based materials, any of a range of metalloids such as silicon, germanium and/or tin, and/or of aluminum, alloys such as lithium titanate and/or possibly composite core-shell particles—having different sizes (e.g., in the order of magnitude of 100 nm, e.g., 100-500 nm, and/or possible in the order of magnitude of 10 nm or 1μ)—for receiving lithiated lithium during charging and releasing lithium ions during discharging. The anodes may further comprise binder(s) and additive(s) as well as optionally coatings (e.g., conductive polymers with or without lithium, conductive fibers such as CNTs (carbon nanotubes) or carbon fibers). Active material particles may be pre-coated by one or more coatings (e.g., by conductive polymers, lithium polymers, etc.), have borate and/or phosphate salt(s) bond to their surface (possibly forming e.g., B₂O₃, P₂O₅), bonding molecules which may interact with the electrolyte and/or various nanoparticles (e.g., boron carbide B₄C, tungsten carbide WC, vanadium carbide, titanium nitride TiN), forming modified anode active material particles, may be attached thereto in anode preparation processes such as ball milling (see, e.g., U.S. Pat. No. 9,406,927, which is incorporated herein by reference in its entirety), slurry formation, spreading of the slurry and drying the spread slurry. Electrolytes may comprise non-aqueous solvents such as mixtures of linear and cyclic carbonate-based solvents and one or more lithium salts, as well as additives. The non-aqueous organic solvent may comprise any of: ester-based solvent(s), ether-based solvent(s), ketone-based solvent(s), alcohol-based solvent(s), and/or aprotic solvent(s), in addition to carbonate-based solvent(s). The lithium salts may be dissolved in the organic solvent(s) and be selected to perform any of the following functions within the battery cells: supply lithium ions in a battery, enable operation of the rechargeable lithium battery, and improve lithium ion transportation between the positive and negative electrodes. Non-limiting examples for lithium electrolyte salt(s) (expressed as Li⁺X⁻ in the electrolyte) may comprise, as respective anions X⁻, any of: F⁻, Cl⁻, Br⁻, I⁻, NO3⁻, N(CN)₂ ⁻, BF₄ ⁻, ClO₄ ⁻, PF₆ ⁻, (CF₃)₂PF₄ ⁻, (CF₃)₃PF₃ ⁻, (CF₃)₄PF₂ ⁻, (CF₃)₅PF⁻, (CF₃)₆P⁻, CF₃SO₃ ⁻, CF₃CF₂SO₃ ⁻, (CF₃SO₂)₂N⁻, (FSO₂)₂N⁻, CF₃CF₂ (CF₃)₂CO⁻, and combinations thereof. The lithium salt(s) may be included in the electrolyte in a concentration of between about 0.1 M to about 2.0 M. The concentration range and values may be selected to optimize the performance and the lithium ion mobility with respect electrolyte conductivity and viscosity. Various additive(s) and their combinations may be added to the electrolyte, such as solid electrolyte interphase (SEI) forming additives, compounds that promote high temperature stability and HF scavengers which prevent battery capacity deterioration. Separator(s) may comprise various materials, such as polyethylene (PE), polypropylene (PP) or other appropriate materials. As non-limiting examples, a polymer membrane such as a polyolefin, polypropylene, or polyethylene membrane, a multi-membrane thereof, a micro-porous film, or a woven or non-woven fabric may be used as the separator.

In the above description, an embodiment is an example or implementation of the invention. The various appearances of “one embodiment”, “an embodiment”, “certain embodiments” or “some embodiments” do not necessarily all refer to the same embodiments. Although various features of the invention may be described in the context of a single embodiment, the features may also be provided separately or in any suitable combination. Conversely, although the invention may be described herein in the context of separate embodiments for clarity, the invention may also be implemented in a single embodiment. Certain embodiments of the invention may include features from different embodiments disclosed above, and certain embodiments may incorporate elements from other embodiments disclosed above. The disclosure of elements of the invention in the context of a specific embodiment is not to be taken as limiting their use in the specific embodiment alone. Furthermore, it is to be understood that the invention can be carried out or practiced in various ways and that the invention can be implemented in certain embodiments other than the ones outlined in the description above.

The invention is not limited to those diagrams or to the corresponding descriptions. For example, flow need not move through each illustrated box or state, or in exactly the same order as illustrated and described. Meanings of technical and scientific terms used herein are to be commonly understood as by one of ordinary skill in the art to which the invention belongs, unless otherwise defined. While the invention has been described with respect to a limited number of embodiments, these should not be construed as limitations on the scope of the invention, but rather as exemplifications of some of the preferred embodiments. Other possible variations, modifications, and applications are also within the scope of the invention. Accordingly, the scope of the invention should not be limited by what has thus far been described, but by the appended claims and their legal equivalents. 

The invention claimed is:
 1. A cathode for fast charging lithium ion cells, the cathode prepared from a cathode formulation comprising: cathode material having spinel or layered structure, olivine-based cathode material, having an olivine-based structure, and being between 5 wt % and 10 wt % of the cathode material, wherein the olivine-based cathode material comprises A_(z)MXO₄, wherein A is Li, alone or partially replaced by at most 10% of Na and/or K; 0<z≤1, M is at least 50% of Fe(II) or Mn(II) or mixture thereof; and XO₄ is PO₄, alone or partially replaced by at most 10 mol % of at least one group selected from the group consisting of SO₄ and SiO₄, binder material, and monomer and/or oligomer material selected to polymerize into a conductive polymer upon partial delithiation of the olivine-based structure cathode material during at least a first charging cycle of a cell having the cathode, wherein the monomer and/or oligomer material comprises monomers and/or oligomers of at least one of pyrrole, aniline, thiophene, phenyl mercaptan, furan, phenol, ethylenedioxythiophene and styrenesulfonate, wherein: the monomer and/or oligomer material is in its pristine form in the cathode prior to the first charging cycle of the cell, the partial delithiation is carried out electrochemically during the first charging cycle of the cell, and during the first charging cycle of the cell, the monomer and/or oligomer material is polymerized; and wherein the partial delithiation increases a capacity of the cathode during fast charging of the fast charging lithium ion cells at rates of 5 C to 15 C.
 2. The cathode of claim 1, wherein the cathode material having spinel or layered structure consists at least one compound selected from the group consisting of: LiNiMnCoO₂, LiNiCoAlO₂, LiMn₂O₄ and LiMn₂NiO₄.
 3. The cathode of claim 1, wherein the olivine-based cathode material comprises LFP (LiFePO₄).
 4. The cathode of claim 1, wherein the cathode material further comprises a carbon coating.
 5. The cathode of claim 1, wherein at least one ring in the monomers and/or oligomers is substituted with one or more straight, branched or bridged alkyl, alkenyl, oxa-alkyl, oxa-alkenyl, aza-alkyl, aza-alkenyl, thia-alkyl, thia-alkenyl, sila-alkyl, sila-alkenyl, aryl, aryl-alkyl, alkyl-aryl, alkenyl-aryl, dialkylamino or dialkylazo group, comprising 1-30 carbon atoms.
 6. The cathode of claim 1, wherein the binder material comprises at least one selected from the group consisting of: carboxymethyl cellulose (CMC), polyvinylidene difluoride (PVDF), polyacrylic acid (PAA), polyethylene oxide (PEO), polyvinyl alcohol (PVA) and alginate.
 7. The cathode of claim 1, comprising 70-90% of cathode material having spinel or layered structure, 5-10% of the olivine-based cathode material, 1-10% of the binder material and 1-10% of the monomer and/or oligomer material.
 8. The cathode of claim 1, comprising 85-93% of the cathode material having spinel or layered structure, 5% of the olivine-based cathode material, 1-5% of the binder material and 1-5% of the monomer and/or oligomer material.
 9. A fast-charging lithium ion cell comprising the cathode of claim
 1. 10. The cathode of claim 1, wherein the partial delithiation increases a capacity of the cathode during fast charging of the fast charging lithium ion cells at rates of 15 C.
 11. The cathode of claim 1, wherein at least one anode of the fast charging lithium ion cells comprises anode material based on at least one compound selected from the group consisting of Si, Ge and Sn.
 12. A fast-charging lithium ion cell comprising: an anode, electrolyte, a separator, and a cathode comprising: cathode material having spinel or layered structure, olivine-based cathode material, having an olivine-based structure, and being between 5 wt % and 10 wt % of the cathode material, wherein the olivine-based cathode material comprises A_(z)MXO₄, wherein A is Li, alone or partially replaced by at most 10% of Na and/or K; 0<z≤1, M is at least 50% of Fe(II) or Mn(II) or mixture thereof; and XO₄ is PO₄, alone or partially replaced by at most 10 mol % of at least one group selected from the group consisting of SO₄ and SiO₄, binder material, and a conductive polymer formed during at least a first charging cycle of the cell from monomer and/or oligomer material selected to polymerize into the conductive polymer upon partial delithiation of the cathode material, wherein the monomer and/or oligomer material comprises monomers and/or oligomers of at least one of pyrrole, aniline, thiophene, phenyl mercaptan, furan, phenol, ethylenedioxythiophene and styrenesulfonate, wherein: the monomer and/or oligomer material is in its pristine form in the cathode prior to the first charging cycle of the cell, the partial delithiation is carried out electrochemically during the first charging cycle of the cell, and during the first charging cycle of the cell, the monomer and/or oligomer material is polymerized; and wherein the partial delithiation increases a capacity of the cathode during fast charging of the fast charging lithium ion cells at rates of 5 C to 15 C.
 13. The fast-charging lithium ion cell of claim 12, wherein the cathode material having spinel or layered structure consists at least one compound selected from the group consisting of: LiNiMnCoO₂, LiNiCoAlO₂, LiMn₂O₄ and LiMn₂NiO₄.
 14. The fast-charging lithium ion cell of claim 12, having a charging curve, in at least a first charging thereof, which comprises a local peak at a specified potential which corresponds to a polymerization reaction of the monomer and/or oligomer material in presence of the partially delithiated olivine-based cathode material.
 15. The fast-charging lithium ion cell of claim 12, wherein the partial delithiation increases a capacity of the cathode during fast charging of the fast charging lithium ion cells at rates of 15 C.
 16. The fast-charging lithium ion cell of claim 12, wherein the anode comprises anode material based on at least one compound selected from the group consisting of Si, Ge and Sn. 